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Multiple Quantum Coherences Hyperpolarized at Ultra-Low Fields.


ABSTRACT: The development of hyperpolarization technologies enabled several yet exotic NMR applications at low and ultra-low fields (ULF), where without hyperpolarization even the detection of a signal from analytes is a challenge. Herein, we present a method for the simultaneous excitation and observation of homo- and heteronuclear multiple quantum coherences (from zero up to the third-order), which give an additional degree of freedom for ULF NMR experiments, where the chemical shift variation is negligible. The approach is based on heteronuclear correlated spectroscopy (COSY); its combination with a phase-cycling scheme allows the selective observation of multiple quantum coherences of different orders. The nonequilibrium spin state and multiple spin orders are generated by signal amplification by reversible exchange (SABRE) and detected at ULF with a superconducting quantum interference device (SQUID)-based NMR system.

SUBMITTER: Buckenmaier K 

PROVIDER: S-EPMC6900040 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Multiple Quantum Coherences Hyperpolarized at Ultra-Low Fields.

Buckenmaier Kai K   Scheffler Klaus K   Plaumann Markus M   Fehling Paul P   Bernarding Johannes J   Rudolph Matthias M   Back Christoph C   Koelle Dieter D   Kleiner Reinhold R   Hövener Jan-Bernd JB   Pravdivtsev Andrey N AN  

Chemphyschem : a European journal of chemical physics and physical chemistry 20191017 21


The development of hyperpolarization technologies enabled several yet exotic NMR applications at low and ultra-low fields (ULF), where without hyperpolarization even the detection of a signal from analytes is a challenge. Herein, we present a method for the simultaneous excitation and observation of homo- and heteronuclear multiple quantum coherences (from zero up to the third-order), which give an additional degree of freedom for ULF NMR experiments, where the chemical shift variation is neglig  ...[more]

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2022-03-31 | GSE195506 | GEO